Substructure Search

19217

COC(=O)C1CCN(C(=O)OC(C)(C)C)CC1
Reaction #8839
title compound
Yield 96.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(=O)n(C)c(C3CCN(C(=O)OCc4ccccc4)CC3)c(-c3ccccc3)c2c1
Reaction #46150
benzyl-4-(6-methoxy-2-methyl-1-oxo-4-phenyl-1,2-dihydroisoquinolin-3-yl)piperidine-1-carboxylate
Yield 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(C(=O)Nc2ccc(Cl)cc2)CC1
Reaction #48551
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(C(=O)Nc2ccc3[nH]ccc3c2)CC1
Reaction #49259
5-[1-(tert-butoxycarbonyl)piperidine-4-carbonylamino]indole
Yield 55.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(C1CCNCC1)N1CCOCC1
Reaction #51234
4-(morpholinocarbonyl)piperidine.hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(CO)CC1
Reaction #52236
l-Boc-piperidine-4-methanol
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(CO)CC1
Reaction #58032
4-Hydroxymethyl-piperidine-1-carboxylic acid tert-butyl ester
Yield 100.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(C(=O)Nc2cccc(Oc3ccc(F)cc3)c2)CC1
Reaction #58160
4-[3-(4-fluoro-phenoxy)-phenylcarbamoyl]-piperidine-1-carboxylic acid tert-butyl ester
Yield 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CNc1ccc(Oc2ccnc(NC(=O)C3CCN(C(=O)OC(C)(C)C)CC3)c2)cc1[N+](=O)[O-]
Reaction #59065
tert-butyl-4-(N-{4-[4-(methylamino)-3-nitrophenoxy]-2-pyridyl}carbamoyl)piperidinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1CCN(C(=O)OC(C)(C)C)CC1
Reaction #60658
title compound
Yield 99.9%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1csc(C2CC[NH2+]CC2)n1.[Cl-]
Reaction #67009
4-(4-Formyl-1,3-thiazol-2-yl)piperidinium chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(C(=O)O[C@H]2CC[C@@]3(C)C(C2)C(=O)C[C@@H]2[C@@H]3CC[C@]3(C)C(=O)CC[C@@H]23)CC1
Reaction #70405
3β-(N-(tert-Butoxycarbonyl)piperidin-4-ylcarbonyloxy)androstane-6,17-dione
Yield 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(C(=O)NCc2n[nH]c3nc(-c4ccc(F)cc4)c(-c4ccncc4)c(-c4ccc(F)cc4)c23)CC1
Reaction #70874
title compound
Yield 26.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(C(=O)NCCn2cc3c(-c4ccc(F)cc4)c(-c4ccncc4)c(-c4ccc(F)cc4)nc3n2)CC1
Reaction #70896
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1C1CCNCC1
Reaction #74586
title compound
Yield 89.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1C1CCN(C(=O)OCc2ccccc2)CC1
Reaction #74587
title compound
Yield 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(CO)CC1
Reaction #78130
title compound
Yield 92.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(C(=O)O)CC1
Reaction #78330
expected product
Yield 95.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1ncc2cc(Nc3nc(-c4cccc(NC(=O)C5CCNCC5)c4)nc4ccccc34)ccc21
Reaction #89843
tert-butyl 5-(2-(3-(piperidine-4-carboxamido)phenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Oc1ccccc1)N1CCC2(CC1)CN(c1ccccc1Cl)c1cc(Cl)ccc12
Reaction #95495
6-chloro-1-(2-chlorophenyl)-1'-phenoxycarbonylspiro[indoline-3,4'-piperidine]
DOI: 10.6084/m9.figshare.5104873.v1
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